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Phase 1 N=9 Treatment

Caffeine for Hypoxic-Ischemic Encephalopathy

Hypoxic-Ischemic Encephalopathy

Enrolled (actual)
9
Serious AEs
29.4%
Results posted
Sep 2024
Primary outcome: Primary: Area Under Plasma Concentration-time at Time t (AUC0-t) for Caffeine — 1137.36; 1177.94; 2213.26; 2768.25 mg*hr/L

Study Design & Population

Study type
Interventional
Phase
Phase 1
Interventions
Caffeine Citrate 5 mg/kg (Drug); Caffeine Citrate 10 mg/kg (Drug)
Age
Pediatric
Sex
All
Sponsor
University of North Carolina, Chapel Hill
Primary completion
Jan 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Area Under Plasma Concentration-time at Time t (AUC0-t) for Caffeine
1137.36; 1177.94; 2213.26; 2768.25
SECONDARY
Number of Participants With Seizures Requiring >1 Anti-Epileptic Medication
1; 0
SECONDARY
Number of Participants With Necrotizing Enterocolitis
0; 0
SECONDARY
Number of Participants With Abnormal MRI Brain Findings Based on NICHD Neonatal Research Network Score
3; 2; 2; 2; 1; 3
SECONDARY
Number of Participants With a Bayley Scales of Infant Development (BSID-III) Cognitive, Language, or Motor Composite Score < 85

Summary

Hypoxic-ischemic encephalopathy (HIE) due to perinatal asphyxia is common and often fatal. Therapeutic hypothermia reduces mortality and morbidity in infants with HIE. Even with the widespread use of therapeutic hypothermia, ~60% of infants with HIE die or have neurodevelopmental impairment. As a result, there is an urgent, unmet public health need to develop adjuvant therapies to improve survival and neurodevelopmental outcomes in this population. Caffeine may offer neuroprotection for infants with HIE by blocking adenosine receptors in the brain and reducing neuronal cell death. In animal models of HIE, caffeine reduces white matter brain injury. Drugs in the same class as caffeine (i.e., methylxanthines) have been shown to be protective against acute kidney injury in the setting of HIE. However, their safety and efficacy have not been studied in the setting of therapeutic hypothermia and their effect on neurological outcomes is not known. Since these drugs reduce injury to the kidney in infants with HIE, they may also reduce injury to the brain. This phase I study will evaluate the pharmacokinetics, safety, and preliminary effectiveness of caffeine as an adjuvant therapy to improve neurodevelopmental outcomes in infants with HIE.

Eligibility Criteria

Inclusion Criteria

  • Documented informed consent from parent or guardian
  • ≥ 36 weeks gestational age at birth
  • Receiving therapeutic hypothermia for a diagnosis of HIE
  • Intravenous (IV) access
  • Postnatal age 1 anti-epileptic drug for seizures
  • Sustained (>4 hours) heart rate > 180 beats per minute
  • Known major congenital anomaly
  • Any condition which would make the participant, in the opinion of the investigator, unsuitable for the study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03913221). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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